Efficacy and safety of low dose Mycophenolate mofetil treatment for immunoglobulin G4-related disease: a randomized clinical trial

Abstract Objectives This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease. Methods Sixty-nine patients newly diagnosed with IgG4-related disease were randomly divide...

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Published inRheumatology (Oxford, England) Vol. 58; no. 1; pp. 52 - 60
Main Authors Yunyun, Fei, Yu, Peng, Panpan, Zhang, Xia, Zhang, Linyi, Peng, Jiaxin, Zhou, Li, Zhang, Shangzhu, Zhang, Jinjing, Liu, Di, Wu, Yamin, Lai, Xiaowei, Liu, Huadan, Xue, Xuan, Zhang, Xiaofeng, Zeng, Fengchun, Zhang, Yan, Zhao, Wen, Zhang
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.01.2019
Oxford Publishing Limited (England)
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Abstract Abstract Objectives This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease. Methods Sixty-nine patients newly diagnosed with IgG4-related disease were randomly divided into two groups (35 patients in Group I and 34 patients in Group II). Patients in Group I received glucocorticoid monotherapy (0.6-0.8 mg/(kg·day) and tapered gradually); patients in Group II received glucocorticoid combined with MMF therapy (1-1.5 g/day). All the patients were followed up at 1, 3, 6 and 12 months. The primary endpoint was response rate in 12 months and the secondary endpoints were relapse, remission rate and adverse reactions. Results Group I and Group II shared almost the same efficacy at the 1 month treatment, but during the follow-up, the complete response rate in Group II was much higher than that in Group I at different time points, and the cumulative relapse rate during 1 year of therapy was much higher in Group I than that in Group II (40.00 vs 20.59%). The remission rate was lower in Group I (51.42 vs 76.47%). Relapses were more likely to happen in lung, lacrimal gland, salivary gland, paranasal sinus and kidney. MMF could reduce relapse, especially organs recurrence. No serious adverse reactions occurred in the two groups. Conclusion Combination treatment with glucocorticoid and MMF was more effective than the monotherapy, and the relapse of IgG4-related disease might be associated with the elevated levels of serum IgG4 and the low glucocorticoid maintenance dose. Trial registration ClinicalTrials.gov, www.clinicaltrials.gov, NCT02458196.
AbstractList This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease.ObjectivesThis randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease.Sixty-nine patients newly diagnosed with IgG4-related disease were randomly divided into two groups (35 patients in Group I and 34 patients in Group II). Patients in Group I received glucocorticoid monotherapy (0.6-0.8 mg/(kg·day) and tapered gradually); patients in Group II received glucocorticoid combined with MMF therapy (1-1.5 g/day). All the patients were followed up at 1, 3, 6 and 12 months. The primary endpoint was response rate in 12 months and the secondary endpoints were relapse, remission rate and adverse reactions.MethodsSixty-nine patients newly diagnosed with IgG4-related disease were randomly divided into two groups (35 patients in Group I and 34 patients in Group II). Patients in Group I received glucocorticoid monotherapy (0.6-0.8 mg/(kg·day) and tapered gradually); patients in Group II received glucocorticoid combined with MMF therapy (1-1.5 g/day). All the patients were followed up at 1, 3, 6 and 12 months. The primary endpoint was response rate in 12 months and the secondary endpoints were relapse, remission rate and adverse reactions.Group I and Group II shared almost the same efficacy at the 1 month treatment, but during the follow-up, the complete response rate in Group II was much higher than that in Group I at different time points, and the cumulative relapse rate during 1 year of therapy was much higher in Group I than that in Group II (40.00 vs 20.59%). The remission rate was lower in Group I (51.42 vs 76.47%). Relapses were more likely to happen in lung, lacrimal gland, salivary gland, paranasal sinus and kidney. MMF could reduce relapse, especially organs recurrence. No serious adverse reactions occurred in the two groups.ResultsGroup I and Group II shared almost the same efficacy at the 1 month treatment, but during the follow-up, the complete response rate in Group II was much higher than that in Group I at different time points, and the cumulative relapse rate during 1 year of therapy was much higher in Group I than that in Group II (40.00 vs 20.59%). The remission rate was lower in Group I (51.42 vs 76.47%). Relapses were more likely to happen in lung, lacrimal gland, salivary gland, paranasal sinus and kidney. MMF could reduce relapse, especially organs recurrence. No serious adverse reactions occurred in the two groups.Combination treatment with glucocorticoid and MMF was more effective than the monotherapy, and the relapse of IgG4-related disease might be associated with the elevated levels of serum IgG4 and the low glucocorticoid maintenance dose.ConclusionCombination treatment with glucocorticoid and MMF was more effective than the monotherapy, and the relapse of IgG4-related disease might be associated with the elevated levels of serum IgG4 and the low glucocorticoid maintenance dose.ClinicalTrials.gov, www.clinicaltrials.gov, NCT02458196.Trial registrationClinicalTrials.gov, www.clinicaltrials.gov, NCT02458196.
Objectives This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease. Methods Sixty-nine patients newly diagnosed with IgG4-related disease were randomly divided into two groups (35 patients in Group I and 34 patients in Group II). Patients in Group I received glucocorticoid monotherapy (0.6–0.8 mg/(kg·day) and tapered gradually); patients in Group II received glucocorticoid combined with MMF therapy (1–1.5 g/day). All the patients were followed up at 1, 3, 6 and 12 months. The primary endpoint was response rate in 12 months and the secondary endpoints were relapse, remission rate and adverse reactions. Results Group I and Group II shared almost the same efficacy at the 1 month treatment, but during the follow-up, the complete response rate in Group II was much higher than that in Group I at different time points, and the cumulative relapse rate during 1 year of therapy was much higher in Group I than that in Group II (40.00 vs 20.59%). The remission rate was lower in Group I (51.42 vs 76.47%). Relapses were more likely to happen in lung, lacrimal gland, salivary gland, paranasal sinus and kidney. MMF could reduce relapse, especially organs recurrence. No serious adverse reactions occurred in the two groups. Conclusion Combination treatment with glucocorticoid and MMF was more effective than the monotherapy, and the relapse of IgG4-related disease might be associated with the elevated levels of serum IgG4 and the low glucocorticoid maintenance dose. Trial registration ClinicalTrials.gov, www.clinicaltrials.gov, NCT02458196.
Abstract Objectives This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease. Methods Sixty-nine patients newly diagnosed with IgG4-related disease were randomly divided into two groups (35 patients in Group I and 34 patients in Group II). Patients in Group I received glucocorticoid monotherapy (0.6-0.8 mg/(kg·day) and tapered gradually); patients in Group II received glucocorticoid combined with MMF therapy (1-1.5 g/day). All the patients were followed up at 1, 3, 6 and 12 months. The primary endpoint was response rate in 12 months and the secondary endpoints were relapse, remission rate and adverse reactions. Results Group I and Group II shared almost the same efficacy at the 1 month treatment, but during the follow-up, the complete response rate in Group II was much higher than that in Group I at different time points, and the cumulative relapse rate during 1 year of therapy was much higher in Group I than that in Group II (40.00 vs 20.59%). The remission rate was lower in Group I (51.42 vs 76.47%). Relapses were more likely to happen in lung, lacrimal gland, salivary gland, paranasal sinus and kidney. MMF could reduce relapse, especially organs recurrence. No serious adverse reactions occurred in the two groups. Conclusion Combination treatment with glucocorticoid and MMF was more effective than the monotherapy, and the relapse of IgG4-related disease might be associated with the elevated levels of serum IgG4 and the low glucocorticoid maintenance dose. Trial registration ClinicalTrials.gov, www.clinicaltrials.gov, NCT02458196.
This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for patients with IgG4-related disease. Sixty-nine patients newly diagnosed with IgG4-related disease were randomly divided into two groups (35 patients in Group I and 34 patients in Group II). Patients in Group I received glucocorticoid monotherapy (0.6-0.8 mg/(kg·day) and tapered gradually); patients in Group II received glucocorticoid combined with MMF therapy (1-1.5 g/day). All the patients were followed up at 1, 3, 6 and 12 months. The primary endpoint was response rate in 12 months and the secondary endpoints were relapse, remission rate and adverse reactions. Group I and Group II shared almost the same efficacy at the 1 month treatment, but during the follow-up, the complete response rate in Group II was much higher than that in Group I at different time points, and the cumulative relapse rate during 1 year of therapy was much higher in Group I than that in Group II (40.00 vs 20.59%). The remission rate was lower in Group I (51.42 vs 76.47%). Relapses were more likely to happen in lung, lacrimal gland, salivary gland, paranasal sinus and kidney. MMF could reduce relapse, especially organs recurrence. No serious adverse reactions occurred in the two groups. Combination treatment with glucocorticoid and MMF was more effective than the monotherapy, and the relapse of IgG4-related disease might be associated with the elevated levels of serum IgG4 and the low glucocorticoid maintenance dose. ClinicalTrials.gov, www.clinicaltrials.gov, NCT02458196.
Author Yu, Peng
Xuan, Zhang
Yamin, Lai
Huadan, Xue
Yunyun, Fei
Linyi, Peng
Li, Zhang
Fengchun, Zhang
Jinjing, Liu
Xiaowei, Liu
Wen, Zhang
Panpan, Zhang
Shangzhu, Zhang
Di, Wu
Xiaofeng, Zeng
Jiaxin, Zhou
Yan, Zhao
Xia, Zhang
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  fullname: Yu, Peng
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Panpan
  fullname: Panpan, Zhang
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  fullname: Xia, Zhang
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Shangzhu
  fullname: Shangzhu, Zhang
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Jinjing
  fullname: Jinjing, Liu
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Di
  fullname: Di, Wu
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Yamin
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  surname: Xiaowei
  fullname: Xiaowei, Liu
  organization: Department of Ophthalmology, Peking Union Medical College Hospital, Beijing, China
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  surname: Huadan
  fullname: Huadan, Xue
  organization: Department of Radiology, Peking Union Medical College Hospital, Beijing, China
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  givenname: Zhang
  surname: Xuan
  fullname: Xuan, Zhang
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Xiaofeng
  fullname: Xiaofeng, Zeng
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  surname: Fengchun
  fullname: Fengchun, Zhang
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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  givenname: Zhao
  surname: Yan
  fullname: Yan, Zhao
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
– sequence: 18
  givenname: Zhang
  surname: Wen
  fullname: Wen, Zhang
  email: Zhangwen91@sina.com
  organization: Department of Rheumatology, Clinical Immunology Center, Peking Union Medical College Hospital, Beijing, China
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ContentType Journal Article
Copyright The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com 2018
The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com
Copyright_xml – notice: The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com 2018
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Keywords glucocorticoid
IgG4-related disease
relapse
response
efficacy
MMF
Language English
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Koizumi ( key 2018121406541975900_key227-B5) 2015; 30
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Snippet Abstract Objectives This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid...
This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid monotherapy for...
Objectives This randomized, controlled clinical trial aims to compare the efficacy and safety of glucocorticoid combined with MMF and glucocorticoid...
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SubjectTerms Autoimmune diseases
Clinical trials
Glucocorticoids
Immunoglobulin G
Immunoglobulin G4
Lacrimal gland and Nasolacrimal duct
Mycophenolate mofetil
Mycophenolic acid
Paranasal sinus
Patients
Remission
Response rates
Salivary gland
Side effects
Sinus
Title Efficacy and safety of low dose Mycophenolate mofetil treatment for immunoglobulin G4-related disease: a randomized clinical trial
URI https://www.ncbi.nlm.nih.gov/pubmed/30124952
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Volume 58
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